Canonical Allele Identifier: CA2259200285
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664985G= , CM000679.2:g.39664985G= GRCh38
NC_000017.10:g.37821238G= , CM000679.1:g.37821238G= GRCh37
NC_000017.9:g.35074764G= NCBI36
NG_008892.1:g.4640G= , LRG_210:g.4640G=
NG_042278.1:g.2005G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-375G= ENSP00000312624.2:n.-375G=